Microfluidic system and method for creating an encapsulated droplet with a removable shell

ABSTRACT

A microfluidic system for creating encapsulated droplets whose shells can be further removed comprises: two electrode plates and a spacing structure disposed between the two electrode plates. One of the electrode plates has three reservoir electrodes and a plurality of channel electrodes. The three electrodes are respectively used for accommodating a shell liquid, a core liquid, and a removing liquid which is able to remove the shell liquid. The channel electrodes are used for communicating droplets among the three reservoir electrodes. Via these arrangements, the microfluidic system can create a quantitative shell droplet and a quantitative core droplet, and then merge the shell and core droplets to form an encapsulated droplet. Moreover, the shell of the encapsulated droplet can be removed by mixing it with the removing liquid. This invention is further provided with a method for creating an encapsulated droplet with a removable shell.

RELATED APPLICATIONS

This application is a Divisional patent application of co-pendingapplication Ser. No. 12/815,580, filed on 15 Jun. 2010, now pending. Theentire disclosure of the prior application, Ser. No. 12/815,580, fromwhich an oath or declaration is supplied, is considered a part of thedisclosure of the accompanying Divisional application and is herebyincorporated by reference.

BACKGROUND OF THE INVENTION

1. Field of the Invention

The present invention relates to an encapsulated droplet, in particular,to a microfluidic system and a method for creating an encapsulateddroplet with a removable shell.

2. Description of Related Art

The microfluidic system, which is also called the microfluidic chip, nowis widely studied and highly valued. It has many advantages, such as,high response rate, high sensitivity, high reproducibility, low cost,and low pollution, so as to be applied to biology, medicine,optoelectronics and other fields.

For the latest technology of the droplet-based microfluidic system, thevolume of the driven droplet has been decreased to the level ofsub-micro liter, or even to the level of pico liter. The rapidevaporation is consequently an issue to the shrunk droplets.

Then, possible solutions to this rapid-evaporation issue includeenhancement of packaging and sealing of the microfluidic system orprecise control of the environmental humidity and temperature. However,the straight forward solutions may increase the systems cost or limitthe applicable situations and environments.

Therefore, some scholars have proposed the concept of encapsulateddroplet by encapsulating the original ease-of-evaporating droplet withanother immiscible droplet. For example, the original one is a waterdroplet; the immiscible one is an oil droplet. The oil droplet will wrapall around the water droplet in order to form an oil shell, preventingthe water drop from evaporation. However, making the oil-shell with acontrolled and reproducible volume by manually dispensing is difficult.

SUMMARY OF THE INVENTION

In view of the above-mentioned issues, a microfluidic system and amethod for creating an encapsulated droplet with a removable shell aredisclosed, in which volume of the encapsulated droplet is able to beprecisely controlled, and the shell droplet of the encapsulated dropletis able to be removed if necessary.

To achieve the above-mentioned objectives, the present inventionprovides a microfluidic system for creating an encapsulated droplet witha removable shell, which includes a first electrode plate, a secondelectrode plate and a spacing structure. The first electrode plate has afirst substrate and a first electrode layer. The first electrode layeris disposed on a surface of the first substrate. The first electrodelayer has a first reservoir electrode, a second reservoir electrode, athird reservoir electrode, a plurality of first channel electrodes beingsequent and adjacent to one another, and a plurality of second channelelectrodes being sequent and adjacent to one another. A respective oneof the first channel electrodes is adjacent to the first reservoirelectrode, while another respective one of those is adjacent to thesecond reservoir electrode. A respective one of the second channelelectrodes is adjacent to the third reservoir electrode, while anotherrespective one of those is adjacent to the first channel electrodes. Thefirst reservoir electrode accommodates a shell liquid, the secondreservoir electrode accommodates a core liquid, and the third reservoirelectrode accommodates a removing liquid that is able to remove theshell liquid. The second electrode plate has a second substrate and asecond electrode layer. The second electrode layer is disposed on asurface of the second substrate and opposite to the first electrodelayer. The spacing structure is disposed between the first and thesecond electrode plates to induce a space formed between the first andthe second electrode plates.

To achieve the above-mentioned objectives, a method for creating anencapsulated droplet with a removable shell is provided. The methodincludes steps as follows: providing a microfluidic system having afirst electrode layer and a second electrode layer opposite to eachother; arranging a shell liquid onto a first reservoir electrode of thefirst electrode layer; arranging a core liquid onto a second reservoirelectrode of the first electrode layer; arranging a removing liquid ontoa third reservoir electrode of the first electrode layer; moving part ofthe shell liquid from the first reservoir electrode to one of channelelectrodes of the first electrode layer by applying an electricpotential across the first and the second electrode layers, so as toform a shell droplet; moving part of the core liquid from the secondreservoir electrode to another one of the channel electrodes of thefirst electrode layer by applying an electric potential across the firstand the second electrode layers, so as to form a core droplet; movingthe shell droplet and the core droplet to contact each other by applyingan electric potential across the first and the second electrode layers,the shell droplet wrapping around the core droplet to form anencapsulated droplet; moving the encapsulated droplet on the channelelectrodes to approach the third reservoir electrode by applying anelectric potential across the first and the second electrode layers; andremoving the shell droplet of the encapsulated droplet by contacting theremoving liquid and the encapsulated droplet.

The present invention further provides a microfluidic system forindividually manipulating multiple liquids to create encapsulateddroplets. The system includes a first electrode plate, a secondelectrode plate and a spacing structure. The first electrode plate has afirst substrate and a first electrode layer. The first electrode layeris disposed on a surface of the first substrate. The first electrodelayer has at least two reservoir electrodes (i.e., first reservoirelectrode and second reservoir electrode), and a plurality of firstchannel electrodes being sequent and adjacent to one another. Arespective one of the first channel electrodes is adjacent to one of thereservoir electrodes, while another respective one of those is adjacentto the other reservoir electrode. The first reservoir electrodeaccommodates a shell liquid, and the second reservoir electrodeaccommodates a core liquid. The second electrode plate has a secondsubstrate and a second electrode layer. The second electrode layer isdisposed on a surface of the second substrate and opposite to the firstelectrode layer. The spacing structure is disposed between the first andthe second electrode plates to induce a space formed between the firstand the second electrode plates.

It is worth mentioning that there are some advantages as follows:

1. Each volume of the shell droplet and the core droplet can bedetermined by the size of the first channel electrode and the distancebetween the first and second electrode plates, so that the volumethereof can be precisely calculated and experimentally obtained withhigh predictability and repeatability.

2. The shell droplet of the encapsulated droplet can be easily removedby merging it with the removing,

in order to further understand the techniques, means and effects thepresent invention takes for achieving the prescribed objectives, thefollowing detailed descriptions and appended drawings are herebyreferred, such that, through which, the purposes, features and aspectsof the present invention can be thoroughly and concretely appreciated;however, the appended drawings are merely provided for reference andillustration, without any intention to he used for limiting the presentinvention.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a cross-sectional view of a microfluidic system for creatingan encapsulated droplet with a removable shell in accordance with apreferred embodiment of the present invention;

FIG. 2 is a top view of a first electrode layer of the microfluidicsystem in accordance with the preferred embodiment of the presentinvention;

FIG. 3 is a top view of a first electrode layer of a microfluidic systemin accordance with another embodiment of the present invention;

FIG. 4 is a top view of a first electrode layer of a microfluidic systemin accordance with an additional embodiment of the present invention;

FIG. 5 is a schematic view illustrating droplets controlled by themicrofluidic system in accordance with the preferred embodiment of thepresent invention;

FIG. 6 is another schematic view illustrating an encapsulated dropletcontrolled by the microfluidic system in accordance with the preferredembodiment of the present invention;

FIG. 7 is a flowchart of a method for creating an encapsulated dropletwith as removable shell in accordance with a preferred embodiment of thepresent invention;

FIGS. 8A to 8F are schematic views illustrating sequential steps of themethod in accordance with the preferred embodiment of the presentinvention;

FIG. 9 is a flowchart of a method in accordance with another embodimentof the present invention;

FIGS. 10A and 10B are schematic views illustrating sequential steps ofthe method in accordance with the other embodiment of the presentinvention.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

Referring now to FIGS. 1 and 2, in which a microfluidic system forcreating an encapsulated droplet with a removable shell in accordancewith a preferred embodiment of the present invention is disclosed. Forconciseness of illustration, the “microfluidic system for creating anencapsulated droplet with a removable shell” is called “microfluidicsystem” for short. The microfluidic system 1 includes a first electrodeplate 11, a second electrode plate 12, and a spacing structure 13. Afterdetailed descriptions for the technical feature of the microfluidicsystem 1, method for using the microfluidic system 1 will be introducedthereby.

The first electrode plate 11 includes a first substrate 111, a firstelectrode layer 112, a dielectric layer 113 and a first hydrophobiclayer 114.

The first substrate 111 can be a rectangular substrate, which is made ofglass materials, silicon materials, poly-dimethylsiloxane (PDMS),polyethylene terephthalate (PET), polyethylene naphthalate (PEN),flexible polymer materials or insulating materials. The glass materialswould be better selections because the low surface roughness thereof mayreduce the driving voltage of the microfluidic system 1.

The first electrode layer 112 is disposed on a surface, a top surface,of the first substrate 111. The first electrode layer 112 is made ofconductive materials, conductive polymeric materials or conductiveoxides, such as Cr, Cu metal, PEDOT: PSS(poly(3,4-ethylenedioxythiophene)polystyrenesulfonate) or Indium TinOxide (ITO). The first electrode layer 112 includes a plurality ofelectrodes 1121 to 1125, which are sequent and adjacent to one another.According to their functional or dimensional requirements, theelectrodes 1121 to 1125 can be divided into a first reservoir electrode1121, a second reservoir electrode 1122, a third reservoir electrode1123, a plurality of first channel electrodes 1124, and a plurality ofsecond channel electrodes 1125.

The first reservoir electrode 1121 is used for reserving a shell liquid2 (shown in FIG. 8). The second reservoir electrode 1122 is used forreserving a core liquid 3, which is immiscible to the shell liquid 2(shown in FIG. 8). The third reservoir electrode 1123 is used forreserving a removing liquid 4, which is able to dissolve the shellliquid 2 but unable to or hard to mix with the core liquid 3 (shown inFIG. 8). The first and second channel electrodes 1124 and 1125 are usedfor communicating the droplets among the three reservoir electrodes 1121to 1123.

The first channel electrodes 1124 could be adjacent to one another in asequential order, i.e. there would he a gap among them, and be arrangedin a horizontal line. Likely, the second channel electrodes 1125 alsoare adjacent to one another in a sequential order, and arranged in avertical line. A respective one of the first channel electrodes 1124,the extreme left one, is adjacent to the first reservoir electrode 1121.Another respective one of the first channel electrodes 1124, the extremeright one, is adjacent to the second reservoir electrode 1122. Arespective one of the second channel electrodes 1125, the extreme bottomone, is adjacent to the third reservoir electrode 1123. Anotherrespective one of the second channel electrodes 1125, the extreme topone, is adjacent to another respective one of the first channelelectrodes 1124, the one next to the extreme right one.

In accordance with the top view of the channel electrodes, the firstchannel electrodes 1124 and the second channel electrodes 1125 arearranged in a form of letter “T”. With respect to FIGS. 3 and 4, thefirst channel electrodes 1124 and the second channel electrodes 1125could also be arranged in forms of letters “E” and “λ”.

With respect to FIG. 2, the top view of each electrode 1121-1125 couldhe rectangular. Moreover, the dimensions of the first, the second andthe third reservoir electrodes 1121-1123 are larger than the dimensionsof the first and the second channel electrodes 1124 and 1125. Therespective three of the first channel electrodes 1124, which are closeto the first reservoir electrode 1121, are denoted as 1124A. Anotherrespective three of the first channel electrodes 1124, which are closeto the second reservoir electrode 1122, are denoted as 1124B. Thedimension of each first channel electrode 1124A could be designed todiffer from that of each first channel electrode 1124B. For example, thedimension of each first channel electrode 1124A is smaller than that ofeach first channel electrode 1124B, so as to change the ratio of shelldroplet to core droplet of the encapsulated droplet mentioned below.

Here are descriptions of other components of the microfluidic system 1.The dielectric layer 113 is disposed on the first electrode layer 112 tocover the electrodes 1121-1125. The dielectric layer 113 could be madeof Parylene, positive photoresist materials, negative photoresistmaterials, high dielectric constant materials, and low dielectricconstant materials.

The first hydrophobic layer 114 is disposed on the top of the dielectriclayer 113 to cover all over the dielectric layer 113. The firsthydrophobic layer 114 is made of hydrophobic materials, such as Teflon,Cytop, and fluoropolymers; and its purpose is to ease the driving of theshell droplet 21 and core droplet 31, (shown in FIG. 5), mentionedbelow. The first hydrophobic layer 114 is also called a low frictionlayer, because of to coefficient of friction between the fluid anditself, so that the fluid can easily flow over the first hydrophobiclayer 114.

The above description is for the first electrode plate 11, and here isdescription for the second electrode plate 12. The second electrodeplate 12 is disposed over and parallel to the first electrode plate 11.The second electrode plate 12 has a second substrate 121, a secondelectrode layer 122 and a second hydrophobic layer 123.

Similarly, the second substrate 121 is a rectangular substrate, whichcould he also made of glass materials, silicon materials, PDMS, PET,PEN, flexible polymer materials or isolating materials. The glassmaterials could be better selections due to the low surface roughnessthereof, which may reduce the driving voltage of the microfluidic system1.

The second electrode layer 122 is disposed on a surface, a bottomsurface, of the second substrate 121, and is opposite to the firstelectrode layer 112. The second electrode layer 122 is made ofconductive materials, conductive, polymeric materials or conductiveoxides, such as Cr, Cu, PEDOT: PSS, metal or ITO.

The second hydrophobic layer 123 is disposed on the bottom of the secondelectrode layer 122 to cover all over the second electrode layer 122.The second hydrophobic layer 123, similar to the first hydrophobic layer114, is made of hydrophobic materials, such as Teflon, Cytop, andfluoropolymers, for easing the driving of the shell droplet 21 and coredroplet 31 (shown in FIG. 5, mentioned below). The second hydrophobiclayer 123 could be also called it low friction layer.

The above description is for the second electrode plate 12, and here isdescription for the spacing structure 13. The spacing structure 13 isdisposed between the first and the second electrode plates 11, 12 toinduce a space 14 formed between the first and the second electrodeplates for accommodating liquid. The spacing structure 13 may be acontinuous frame structure or several separated pillar structures.

The fluid in the microfluidic system 1 is controlled through physicalphenomena, such as Dielectrophoresis (DEP), Electrowetting-on-dielectric(EWOD), in accordance with the properties of the liquid, such asdielectric fluid or conductive fluid. Usually, dielectric fluid isnon-polar liquids; the conductive fluid is polar liquids. If the liquidis a dielectric fluid, it may be driven by the phenomenon of DEP. If theliquid is a conductive fluid, the liquid may be driven by the phenomenonof EWOD or DEP.

With respect to FIGS. 5 and 6, more details regarding how themicrofluidic system 1 controls the fluid or droplet and creates theencapsulated droplet are described below. A shell droplet 21 and a coredroplet 31 are taken as an example.

The shell droplet 21 is a dielectric fluid, such as an oil droplet,arranged in the space 14 and on a respective one of the first channelelectrodes 1124A. The core droplet 31 is a conductive fluid, such as awater droplet, arranged in the space 14 and on a respective one of thefirst channel electrodes 1124B. The shell droplet 21 and the coredroplet 31 are individually surrounded by environmental fluid, such asair.

With respect to FIG. 5, a direct current (DC) is applied between thesecond electrode layer 122 and a respective one of the first channelelectrodes 1124A, which is just at the right hand side of the shelldroplet 21. Due to the difference of the dielectric constant between theshell droplet 21 and the air, different electric forces on the interfacewill generate a pressure difference, which leads the shell droplet 21 tomove toward the right hand side. The phenomenon is called DEP. Analternating, current (AC)is applied between the second electrode layer122 and a respective one of the first channel electrodes 1124B, which isjust at the left hand side of the core droplet 31. Due to the decreaseof the contact angle between the core droplet 31 and the dielectriclayer and/or hydrophobic layer, a pressure difference is generated so asto lead the core droplet 31 to move forward the left-hand side, wherethe liquid pressure is smaller. The phenomenon is called EWOD.

FIG. 6 illustrates the encapsulated droplet, which is formed by the coredroplet 31 wrapped in the shell droplet 21 spontaneously due todifferent surface tensions when they contact. Because the encapsulateddroplet possesses dielectric and conductive fluids. DEP and EWOD wouldhe chosen for the movement of the encapsulated droplet. The EWODphenomenon is selected to implement in the preferred embodiment.Moreover, the core droplet 31 in FIG. 5 can also be driven through theDEP phenomenon, which is usually induced by a DC signal. However, theDEP phenomenon can also be induced by an AC signal.

Referring to FIGS. 7 and 8, a method for creating an encapsulateddroplet with a removable shell according to a preferred embodiment ofthe present invention is described below, which is performed by themicrofluidic system 1 mentioned above.

Referred in step S101: a microfluidic system 1 is provided, and a shellliquid 2, a core liquid 3 and a removing liquid 4 are selected to use inthe microfluidic system 1. The shell liquid 2 and the core liquid 3 maybe respectively dielectric fluid and conductive fluid depending on thespecific function that the microfluidic system 1 meets. In thisembodiment, the dielectric fluid, such as silicone oil, which isbeneficial to the biomedical field very well, is selected as the shellliquid 2; the conductive fluid, such as water, is selected as the coreliquid 3; and the volatile solvent, such as Hexane, which can mix withand dissolve the silicone oil very well, is selected as the removingliquid.

Referred in steps S103 to S107: shown in FIG. 8A, the shell liquid 2 isarranged in the space 14 and on the first reservoir electrode 1121, thecore liquid 3 is arranged in the space 14 and on the second reservoirelectrode 1122, and the removing liquid 4 is arranged in the space 14and on the third reservoir electrode 1123. Proper electric potentialsare applied to the first, second and the third reservoir electrodes1121, 1122 and 1123 to hold liquid 2, 3, and 4 thereon respectively.

Referred in step S109: shown in FIG. 8B, the electric potential isapplied to the second electrode layer 122 and a respective one of thefirst channel electrodes 1124A, which is closest to the first reservoirelectrode 1121. Part of the shell liquid 2 can be moved by DEP to theone of the first channel electrodes 1124A, to which electric potentialis applied, so as to form a shell droplet 21.

Referred in step S111: shown in FIG. 8C, the electric potential isapplied to the second electrode layer 122 and a respective one of thefirst channel electrodes 1124B, which is closest to the second reservoirelectrode 1122. Part of the core liquid 3, can be moved by EWOD to theone of the first channel electrodes 1124B, to which electric potentialis applied, so as to form a core droplet 31.

Referred in step S113: shown in FIGS. 8D and 5, the electric potentialis applied to the first channel electrodes 1124A and the secondelectrode layer 122: and the electric potential is applied to the firstchannel electrodes 1124B and the second electrode layer 122. Therefore,the shell droplet 31 and the core droplet 21 move respectively on thefirst channel electrodes 1124A and 1124B so as to contact or merge witheach other. The shell droplet 21 wraps around the core droplet 31 toform an encapsulated droplet.

Referred in step S115: shown in FIG. 8E, the electric potential isapplied to the second channel electrodes 1125 and the second electrodelayer 122, so as to move the encapsulated droplet on the second channelelectrodes 1125 until it approaches the third reservoir electrode 1123.

Referred in step S117: shown in FIG. 8F, the removing liquid 4 on thethird reservoir electrode 1123 contacts the shell droplet 21 of theencapsulated droplet. The removing liquid 4 mixes with the shell liquid21, and dissolves the shell liquid 21, so that the encapsulated dropletis returned to the core droplet 31. Then, the electric potential isapplied to the second channel electrodes 1125 and the second electrodelayer 122 again, making the core droplet 31 leave the third reservoirelectrode 1123 to one of the second channel electrodes 1125. A part ofthe removing liquid 4 is also moved to the second channel electrode 1125with core droplet 31, and wraps around the core droplet 31. However, theremoving liquid 4 evaporates in a short period of time, leaving the coredroplet 31 alone on the second channel electrode 1125.

The procedures of steps S101 to S117 can be adjusted. For example, thestep S107 can be set following the step S115, and the step S109 can beset following the step S111. The result of the adjusted steps is as sameas the previous one.

Moreover, after the step S113, a second shell droplet (not shown) can befurther formed, to be immiscible with the shell droplet 21. The secondshell droplet contacts the encapsulated droplet to create a second shellthereon. To repeat this step, the encapsulated droplet could havemultiple shells thereon.

By the method of creating the encapsulated droplet, the volume of shelldroplet 21 or the core droplet 31 can be calculated precisely. Thevolume is obtained in response to the dimension of each first channelelectrode 1124A, 1124B and the distance between the first and the secondelectrode plates 11 and 12. When the dimension of each first channelelectrode 1124A and 1124B is larger, the volume of the shell droplet 21and the core droplet 31 become greater.

In addition to increasing the dimension of the first channel electrodes1124A and 1124B, the volume of the shell droplet 21 and the core droplet31 could be increased further by the steps mentioned below. With respectto FIGS. 9 and 10, the shell droplet 21 is taken as an example.

Referred in step S201: with respect to FIG. 10A, the shell droplet 21has been formed on a respective one of the first channel electrodes1124A, which is remote from the first reservoir electrode 1121. Thenelectric potential is applied to the second electrode layer 122 andanother respective one of the first channel electrodes 1124A, which isclose to the first reservoir electrode 1121. Another partial part of theshell liquid 2 can move to the first channel electrode 1124A, to whichthe electric potential is applied, so as to form another shell droplet21A.

Referred in step S203: with respect with FIG. 10B, the electricpotential is applied to the first channel electrodes 1124A and thesecond electrode layer 122. Then the two shell droplets 21 and 21A moveon the first channel electrode 1124A to contact each other. The twoshell droplets 21, 21A merge with each other to create a lamer shelldroplet 21B.

After the step S203, the step S113 may be performed to form theencapsulated droplet having a larger quantitative shell droplet 21B.Moreover, it is noteworthy that the steps S201 and S203 can be repeatedmore than once, so as to further increase the volume of shell droplet21B.

Here are descriptions for real applications of the microfluidic system1, such as extraction, purification, protein crystallization, andartificial cell membrane formation. Take extraction fur instance, whilethe user injects the blood sample into the shell liquid 2, the coreliquid 3 attracts a specific molecule of the blood sample. When theshell droplet 21 containing the specific molecule of the blood samplecontacts the core droplet 31 to create an encapsulated droplet, thespecific molecule of the blood sample will move into the core droplet31. Alter the shell droplet 21 is removed by the removing liquid 4, thecore droplet 31 only includes one specific molecule of the blood sample,so as to achieve the extraction. In addition, the volume of the shelldroplet 21 and the core droplet 31 could be calculated, so that theconcentration of the extracted molecule is calculated thereby.

Take purification for instance, while the user injects the blood sampleinto the core liquid 3, the shell liquid 2 attracts a specific moleculeof the blood sample. When the core droplet 31 containing the specificmolecule of the blood sample contacts the shell droplet 21 to create anencapsulated droplet, the specific molecule of the blood sample will bemoved into the shell droplet 21. After the shell droplet 21 is removedby the removing liquid 4, the core droplet 31 would not include thespecific molecule of the blood sample, so as to achieve thepurification.

Take protein crystallization for instance, while the user injects theprotein molecules into the core liquid 3, the core droplet 31 mergeswith the shell droplet 21 to create an encapsulated droplet includingthe protein molecules. Because the vaporization velocity of core droplet31 could be controlled in the encapsulated droplet, which is adjusted bythe types and volume of the shell droplet 21, the protein crystal growthand nucleation would be controlled in accordance with the vaporizationvelocity. Therefore, the protein molecules arrange in order slowly forcrystallization.

Take artificial cell membrane formation for instance, while the userinjects lipid molecules into the core liquid 3 or the shell liquid 2,the core droplet 31 merges with the shell droplet 21 to create anencapsulated droplet with a monolayer of lipid molecules self-assembledat the core-shell liquid interface. When contact two or moreencapsulated droplets, artificial cell membrane(s) can be formed betweentwo encapsulated droplets.

Other embodiments of the microfluidic system 1 are detailed below. Ifthe shell liquid 2 or the core liquid 3 possesses sufficient hydrophobicproperty or surface energy, or the dielectric layer 113 and the secondelectrode layer 122 are hydrophobic to the shell liquid 21 or the coreliquid 3, the first hydrophobic layer 114 and the second hydrophobic 123are not necessary to be set.

Moreover, if the shell liquid 21 and the core liquid 31 are bothcontrolled through the DEP phenomenon, and the dielectric property ofthe shell liquid 2 and the core liquid 3 has met usage requirements, thedielectric layer 113 are not necessary to be set.

Moreover, the second electrode layer 122 may include individualsequential electrodes, and the dimension and arrangement of eachelectrode would correspond to the electrodes 1221 to 1125 of the firstelectrode layer 112.

Furthermore, the shell liquid 2 and the core liquid 3 could he theconductive fluid or polar liquid. For example, the shell liquid 2 can behigh-carbon aliphatic alcohol, such as octanol or decanol alcohol, whilethe core liquid 2 is water.

In conclusion, it is worth mentioning that there are some advantages asfollows:

1. Each volume of the shell droplet 21 and the core droplet 31 isdetermined in response to the size of the first channel electrode 1124and the distance between the first and second electrode plates 11, 12,so that the volume thereof can be calculated precisely and obtained withhigh predictability and repeatability.

2. The shell droplet 21 of the encapsulated droplet can be easilyremoved by merging with the removing liquid 4.

The above-mentioned descriptions represent merely the preferredembodiment Of the present invention, without any intention to limit thescope of the present invention thereto. Various equivalent changes,alternations or modifications based on the claims of present inventionare all consequently viewed as being embraced by the scope of thepresent invention.

1. A microfluidic system for creating an encapsulated droplet with aremovable shell comprising: a first electrode plate having a firstsubstrate and a first electrode layer, the first electrode layer beingdisposed on a surface of the first substrate, the first electrode layerhaving a first reservoir electrode, a second reservoir electrode, athird reservoir electrode, a plurality of first channel electrodes beingsequent and adjacent to one another, and a plurality of second channelelectrodes being sequent and adjacent to one another, one of the firstchannel electrodes being adjacent to the first reservoir electrode,another one of the first channel electrodes being adjacent to the secondreservoir electrode, one of the second channel electrodes being adjacentto the third reservoir electrode, another one of the second channelelectrodes being adjacent to the first channel electrodes, the firstreservoir electrode being used for accommodating a shell liquid, thesecond reservoir electrode being used for accommodating a core liquid,and the third reservoir electrode being used for accommodating aremoving liquid capable of removing the shell liquid; a second electrodeplate having a second substrate and a second electrode layer, the secondelectrode layer being disposed on a surface of the second substrate andopposite to the first electrode layer; and a spacing structure disposedbetween the first and the second electrode plates, wherein a space isformed between the first and the second electrode plates.
 2. Themicrofluidic system according to claim 1, wherein the shell liquid orthe core liquid is a dielectric fluid.
 3. The microfluidic systemaccording to claim 1, wherein the shell liquid or the core liquid is aconductive fluid.
 4. The microfluidic system according to claim 1,wherein the first electrode plate includes a dielectric layer disposedon the first electrode layer.
 5. The microfluidic system according toclaim 4, wherein the first electrode plate includes a hydrophobic layerdisposed on the dielectric layer.
 6. The microfluidic system accordingto claim 1, wherein the second electrode plate includes a hydrophobiclayer disposed on the second electrode layer.
 7. The microfluidic systemaccording to claim 1, wherein the first channel electrodes and thesecond channel electrodes are arranged in forms of letters “T”, “λ” or“E”.
 8. The microfluidic system according to claim 1, wherein the firstand the second substrates are made of glass materials.
 9. A microfluidicsystem for creating an encapsulated droplet with a removable shellcomprising: a first electrode plate having a first substrate and a firstelectrode layer, the first electrode layer being disposed on a surfaceof the first substrate, the first electrode layer having a firstreservoir electrode, a second reservoir electrode, a plurality of firstchannel electrodes being sequent and adjacent to one another, one of thefirst channel electrodes being adjacent to the first reservoirelectrode, another one of the first channel electrodes being adjacent tothe second reservoir electrode, the first reservoir electrode being usedfor accommodating a shell liquid, the second reservoir electrode beingused for accommodating a core liquid; a second electrode plate having asecond substrate and a second electrode layer, the second electrodelayer being disposed on a surface of the second substrate and oppositeto the first electrode layer; and a spacing structure disposed betweenthe first and the second electrode pates, wherein a space is formedbetween the first and the second electrode plates.